A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020794



Internal ID21930137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26289541..26290661hg38UCSC Ensembl
chr11:26311088..26312208hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020794
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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